A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634347



Internal ID7021150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:45354869..45554117hg38UCSC Ensembl
chr14:45824072..46023320hg19UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38199249
hg19199249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15002663, essv15002657, essv15002668, essv15002653, essv15002659, essv15002669, essv15002658, essv15002660, essv15002667, essv15002665, essv15002662, essv15002656, essv15002654, essv15002664, essv15002666, essv15002655, essv15002652, essv15002661
SamplesNA19701, HG02583, NA18878, HG02489, HG02281, HG03212, NA19209, NA19200, NA18933, NA18871, NA18907, NA19149, HG02308, NA19473, HG02923, HG03304, NA19351, HG03351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634347
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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